VIRGILIO, ROBERTA
VIRGILIO, ROBERTA
DIPARTIMENTO DI SCIENZE NEUROLOGICHE (attivo dal 01/01/2001 al 27/04/2012)
The m.12316G>A mutation in the mitochondrial tRNA Leu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment
2010 D. Ronchi, R. Virgilio, A. Bordoni, E. Fassone, M. Sciacco, P. Ciscato, M. Moggio, A. Govoni, S. Corti, N. Bresolin, G.P. Comi
Transplantation of neural stem cells derived from engineered ESC lineage (sox2-βgeo/oct4-tk cells) improves the phenotype of a mouse model of Spinal Muscular Atrophy
2009 S. Corti, M. Nizzardo, M. Nardini, S. Salani, C. Donadoni, D. Ronchi, D. Papadimitriou, R. Virgilio, N. Bresolin, G. Comi
Molecular epidemiology and clinical features of a large Italian cohort of 291 dystrophinopathic patients.
2009 F. Magri, A. Govoni, M.G. D’Angelo, R. Del Bo, S. Tedeschi, S. Ghezzi, R. Virgilio, S. Bonato, S. Gandossini, A. Bordoni, S. Corti, V. Crugnola, A. Prelle, C. Lamperti, M. Moggio, N. Bresolin, G.P. Comi
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodies
2009 R. Virgilio, S.P. Corti, P. Agazzi, D. Santoro, S. Lanfranconi, L. Candelise, N. Bresolin, G.P. Comi, A. Bersano
Inclusion body myopathy and frontotemporal dementia caused by a novel VCP mutation
2009 A. Bersano, R. Del Bo, C. Lamperti, S. Ghezzi, G. Fagiolari, F. Fortunato, E. Ballabio, M. Moggio, L. Candelise, D. Galimberti, R. Virgilio, S. Lanfranconi, Y. Torrente, M. Carpo, N. Bresolin, G.P. Comi, S. Corti
Mitochondrial DNA G8363A mutation in the tRNA Lys gene: clinical, biochemical and pathological study
2009 R. Virgilio, D. Ronchi, A. Bordoni, E. Fassone, S. Bonato, C. Donadoni, G. Torgano, M. Moggio, S. Corti, N. Bresolin, G.P. Comi
Comprehensive genetic analysis and clinical follow-up findings in 203 DMD patients
2008 R. Virgilio, F. Magri, R. Del Bo, S. Ghezzi, S. Tedeschi, M.G. D’Angelo, D. Coviello, A. Prelle, A. Bordoni, M. Sciacco, C. Lamperti, S. Corti, Y. Torrente, M. Moggio, N. Bresolin, G.P. Comi
Stop codons, duplicazioni e delezioni: caratterizzazione genetica e follow-up clinico in una coorte di 201 pazienti affetti da distrofia Muscolare di Duchenne
2008 F. Magri, R. Virgilio, R. Del Bo, S. Ghezzi, S. Tedeschi, M.G. D’Angelo, D. Coviello, A. Prelle, A. Bordoni, M. Sciacco, C. Lamperti, S. Corti, Y. Torrente, M. Moggio, N. Bresolin, G.P. Comi
A stop codon mutation in the 5’ of the dystrophin gene associated to a Becker muscular dystrophy phenotype
2008 F. Magri, R. Virgilio, R. Del Bo, F. Fortunato, S. Ghezzi, R. Cagliani, M. Sironi, M.G. D'Angelo, V. Crugnola, M. Moggio, N. Bresolin, G.P. Comi
Mitochondrial DNA G8363A mutation in the tRNA Lys gene : clinical features of a new family
2008 R. Virgilio, D. Ronchi, A. Bordoni, E. Fassone, M. Moggio, S. Bonato, G. Conti, C. Donadoni, L. Barbetta, G. Torgano, S. Corti, N. Bresolin, G.P. Comi
Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia
2008 R. Virgilio, D. Ronchi, G.M. Hadjigeorgiou, A. Bordoni, F. Saladino, M. Moggio, L. Adobbati, D. Kafetsouli, E. Tsironi, S. Previtali, A. Papadimitriou, N. Bresolin, G.P. Comi
Clinical features of an adult-onset Leigh syndrome caused by the T9176C mutation in the mitochondrial DNA ATPase 6 gene
2008 D. Ronchi, A. Bordoni, R. Virgilio, E. Fassone, A. DiFonzo, M. Servida, M. Ronconi, V. Lucchini, M. Matteoli, N. Bresolin, G.P. Comi
Mitochondrial DNA microarray resequencing in Leber's hereditary optic neuropathy and other mitochondrial encephalomyopathies
2007 F. Saladino, R. Virgilio, I. Cifola, A. Bordoni, S. Galbiati, C. Battaglia, N. Bresolin, G.P. Comi
Muscle mitochondrial oxidative defects in Amyotrophic Lateral Scelosis
2007 V. Crugnola, V. Lucchini, S. Corti, L. Adobbati, A. Ciammola, N. Ticozzi, M.E. Fruguglietti, A. Prelle, D. Santoro, R. Virgilio, V. Silani, N. Bresolin, M. Moggio, G.P. Comi
A novel mutation in the mitochondrial tRNA LeuCUN gene associated with a mitochondrial myopathy with respiratory impairment
2007 R. Virgilio, A. Bordoni, D. Ronchi, F. Saladino, N. Bresolin, M. Sciacco, G.P. Comi
Screening of mitochondrial myopathy with mtDNA multiple deletions and characterization of patients without mutations in known loci
2006 R. Virgilio, D. Ronchi, A. Bordoni, L. Adobbati, G.M. Hadjigeorgiou, F. Saladino, A. Papadimitriou, M. Moggio, N. Bresolin, G.P. Comi
Screening of Twinkle gene in POLG1- and ANT1-negative patients with mitochondrial myopathy and multiple mitochondrial DNA deletions : four new mutations
2006 R. Virgilio, D. Ronchi, A. Bordoni, L. Adobbati, G.M. Hadjigeorgiou, D. Kafetsouli, E. Tsironi, A. Papadimitriou, M. Moggio, N. Bresolin, G.P. Comi
New twinkle gene mutations in PEO patients with multiple mitochondrial DNA deletions
2006 R. Virgilio, A. Bordoni, D. Ronchi, G.M. Hadjigeorgiou, R. Del Bo, V. Crugnola, D. Kafetsouli, E. Tsironi, A. Papadimitriou, N. Bresolin, G.P. Comi
Association between VEGF gene and sporadic Alzheimer’s Disease
2005 R. Del Bo, M. Scarlato, S. Ghezzi, F. Martinelli Boneschi, C. Fenoglio, S. Galbiati, R. Virgilio, D. Galimberti, G. Galimberti, M. Crimi, C. Ferrarese, E. Scarpini, N. Bresolin, G.P. Comi
Influence of the Glu298Asp polymorphism of NOS3 on age at onset and homocysteine levels in AD patients
2005 I. Guidi, D. Galimberti, E. Venturelli, C. Lovati, R. Del Bo, C. Fenoglio, A. Gatti, R. Dominici, S. Galbiati, R. Virgilio, S. Pomati, G.P. Comi, C. Mariani, G. Forloni, N. Bresolin, E.A. Scarpini